Int J Pharm Pharm Sci, Vol 9, Issue 10, 260-264Original Article


ANTICLASTOGENICITY OFTINOSPORA CORDIFOLIA STEM EXTRACT AGAINST ARSENIC GENOTOXICITY IN MUS MUSCULUS BONE MARROW ERYTHROCYTES USING MICRONUCLEUS ASSAY

SK. AMBASTA1*, S. KUMARI2, UK. SINHA1

1Department of Botany (Biotechnology),Faculty of Science, Patna University, Patna, Bihar, India, 2Department of Biotechnology, Faculty of Science, Utkal University, Bhubaneswar, Odisha, India
Email: ambasta.2017@gmail.com

Received: 25 May 2017 Revised and Accepted: 31 Aug 2017


ABSTRACT

Objective: The study was aimed to evaluate anticlastogenic potential of ethanolic extract of T. cordifoliastem against arsenic induced genotoxicity.

Methods: In the experiment twenty five animals were taken and divided into five groups and each group contain five animals. Group 01(control) and fed on tap waterwhile the rest four (02, 03, 04, 05) groups were treated with 4 mg/kg body weight, per orally sodium arsenite for 8 w.Sodium arsenite pretreated groups04 and 05 were followed bydose of 80 mg/kg body weight of 5% ethanolic solution of the test plant stem extract for a next 8 w. Bone marrow cells were collected in Hank’s Balanced Salt Solution and smearedon a slide followed by double staining (Giemsa and Harris hematoxylin).

Results: High index of micronucleus frequency was observed in the groups 02 and 03 in contrast to group 01(control) while micronucleus frequency dramatically reduced in 04 and 05 groups. The mean number of micronucleus scored/2000 cell was found to be 2.6, 19.2, 20.2, 7 and 6.8 in group 01, 02, 03, 04, 05 respectively. Arsenic treated mice (03) showed remarkable increase (p≤0.001)in micronucleus frequency when compared to the corresponding values for control group (01). The percentage micronucleus frequency (mean and standard deviation) was markedly decreased(p0.019) when group 04 was compared with arsenic treated animals (group 02) and (p0.001) while group 05 was compared with arsenic treated animals (group 03) for their corresponding values.

Conclusion: The findings of this study have shown that T. cordifolia may be used as a preventive herbal drug against chemical or arsenical toxicity which leads to damage of genetic materials.

Keywords: Acentromeric, Mitotic apparatus, Genotoxicity


INTRODUCTION

Micronucleus (MN) assay is used in the genotoxicological screening and it is anexcellent biomarker of genetic damage[1]. In the cell MNmay be induced from clastogens or an aneugens (an agent that induces chromosomal loss mainly through interference with spindle apparatus or mitotic apparatus) [2].It is a chromatin containing body which may represent acentromeric fragments of chromosome or whole chromosome, which unable to get incorporated in the daughter cell at cell division [3]. MN assay is rapid, easy, cheap and sensitive tool for detection of mutagens [4]. TheMN index in rodents or human cell is used in the assessment of genotoxicity in vivo or ex-vivo [5]. In the micro nucleated cells, micronuclei have diameter ≤ 1/3 of intact nucleus and may stained lighter or equal to parent nucleus [6]. The bone marrow cytogenetic study is a short term technique for unrolling the mechanism which is involved in clastogenic and anticlastgenic activities of mutagens[7].

Arsenic contamination of the biosphere from geological as well as anthropogenic sources is a significant environmental health concern[8]. It is highly genotoxic and its toxicity depends on physical states, oxidative state,rate of elimination and absorption and their extent of exposure. Arsenic and its compounds replaces phosphorous from thephosphodiester bond of DNA and forms arsenodiester bond which causes clastogenicity andalso impairs the DNA repair mechanism[9]. Arsenical induces oxidative stress and generates reactive oxygen species (ROS), which leads to DNA damage[10]. Medicinal plants are an important and analternative sourceto extract natural antioxidant compounds to delay or prevent the oxidative damage caused by ROS [11]. Generation of reactive oxygen species during biotransformation of arsenicals inside the living cells mainly concerned with chromosomal aberrations or DNA damage [12].

T. cordifolia belongs to family menispermaceae and it is adeciduous climbing shrub occurs in the entire partsof India, especially in the tropical region at analtitude of 3000 meters [13].Various studies have shown that the test plant has anticancer activity as well as it significantly reduces the MN formation [14].T. cordifolia has little or no adverse effect regarding its cellular toxicity [15]. A lot of research papers have illustrated that some phenolic compounds ofT. cordifolia has anti-carcinogenic potential and anti-mutagenic activity [16]. Phenolic compounds are chief bioactive compounds of many plants which bear potent antioxidant properties that show the modulatory effects on physiological redox reactions [17].It is evident that ethanolic extract of medicinalplants mayhave an antagonisticeffect towards the oxidative stress caused due to arsenics[18].

In the present study anticlastgenicor anti-genotoxic effects of test plant stem extract was investigated against arsenical genotoxicity in bone marrow erythrocytes of Swiss albino mice by using the micronucleus assay technique.

MATERIALS AND METHODS

Experimental animal

Physiologically healthy Swiss mice were selected and housed under good hygienic condition. They were allowed to acclimatize for 15 d under controlled condition of illumination (a 12 h light: dark cycle) and temperature 22-25 °C. The animals were maintained on a standard pellet dietand green vegetables. Huskbeddingwas provided to animals throughout the experiment and the present study was approved by the Institutional Animal Ethics Committee(Sanction No: 2017/1B-10/08/17).

Chemicals

Sodium arsenite (Sigma, CAS: 7784-46-5),Giemsa stain solution (Sigma, CAS: 51811-82-6), Harris Hematoxylin (Sigma, CAS: 517-28-2)), Ethanol (Sigma, CAS: 64-17-5), Methanol (Scientific Fischer, CAS: 67-58-1), Glacial acetic acid (Merck, CAS: 64-19-7). All chemicals used in the experiment are of analytical grade, were purchased from local supplier (Bihar Scientific Chemicals, Ashok Raj Path, Patna, India).

Extract preparation of the test plant material

The test plant was collected from thedepartmental glass house of botany, Patna University and Patna(Bihar). The plant was identified and authenticated; a voucher specimen (TNB/60/2014) has been deposited in the post graduate department of botany, Patna University, Patna for future reference. The departmental glass house is locatednear the Ganga bank at longitude of 85 °10̕ E and latitude 25 °36̛ N. Test plant was growninearthen pot filled with garden soil (loamy), mixed with organic fertilizers.The stem (100 g) of healthy T. cordifoliawas washed with running tap water properly to remove dirt and other contaminating agents and allowed to dry at 40 °C for 14-15 d in hot air woven. The dried plant material (0.5-1% moisture content) was milled into fine powder and dissolved in 90 % ethanoland the suspension was placed on horizontal shaker for 24 h for their complete dissolution. The mixture was then subjected to separation of extractby vacuum rotavator (Buchi, R-3) at bath temperature 55 ° C, rotation 6 rpm and pressure was maintained at 310 milli bar. The extract was evaporated till totheir dryness and obtained extract product was stored in refrigerator at 4 °C for future use.

Herbal dose preparation of test plant extract

Every day fresh herbal dose was prepared prior to their administration to the experimental animals. Dose was prepared by dilution of crude extract of T. cordifolia in 5% ethanol which was vigorously shacked for 2-3 min to their mixing. The suspension was then filtered by what-man filter paper 01 (Cat No: 1001110) of pore size 110 nm to eliminate larger or non-dissolved particles from mixture.

Experimental design

Double staining (Giemsa and Harris Hematoxylin) procedure was used in this study.Double staining enhances the clarity of micronucleus and increases the scoring time. The experimental mice were divided into five groups and each group comprising five animals. Each cage was numerically marked as01, 02, 03, 04, and 05 for their group categorization. Animals of group 01(control) was fed with clean tap water supply of Patna city, India.Animalsof group 02, 03, 04, 05 were received sodium arsenite at the rate of 4 mg/kg body weight, per orally for 08 w. After completion of sodiumarsenite treatment,groups 04 and 05 (sodium arsenite pretreated) wereadministrated with herbaldose of 80 mg/kg body weight, per orally test plant stem extract for next 08 w (total duration oftreatment was 16 w). The treatment (sodium arsenite and herbal extract) were given to each individualmice of each group strictly with an accordance of their body weight, daily once. Randomly two animals were picked from each animal group and sacrificed by their cervical dislocation.The hind limbs were surgically removed and adhered tissue was cleaned off by surgical blade. Both ends of femur bone were opened by making fine nick to their terminal edge. The marrow was flushed out in the test tube by means of syringe containing 3 ml of sterilized and refrigerated Hank Balanced Salt Solution.Such solution was maintained at physiological pH (7.4)and isotonic with to bone marrow cells and without phenol red.Collected bone marrow cells in the solution were subjected to make a homogeneous suspension with the help of pipette and this homogenate was allowed to centrifuged (Ependorff 5810R) at 1000 rpm for 5 min. Supernatant was removed and cell pellet or button was mixed by aspiration and re-centrifuged at same rpm and period. Such cycle was repeated for three times.

Slide preparation and staining

Small drop of viscous suspensionwas smeared on surface sterilized glass slide (Blue star industries) of dimension 75 mm × 25 mm × 1.35 mm with variation in thickness±0.1mm.Slides were dried at temperature 40 °C for few minutes and subsequently submerged into 100% chilled methanol for fixing of bone marrow cells for 10 min. The fixed bone marrow erythrocytes were stained with Harris hematoxylin mixed with 3.5 % Glacial acetic acid for 10 min. Glacial acetic acid improves the specificity of chromatin material.Harris hematoxylin stained slides were then stained with 1/9 diluted Giemsa stain for 10 min.Excess stainwas removed by dipping of slides into cold distilled water and slides were kept vertical on blotting paper for few seconds to absorb water and their undersides were wiped out. Micronuclei were scored by two different observers to minimize error and2000(approx) cells were observed with light microscope (Olympus) under 10 × 100 × magnification. The frequency of MN in femoral bone cells were evaluated according to procedure of Schmid [19], with some modifications as reported [20].

Statistical analysis

The data of micronucleus frequency (%) were expressed in the terms of mean±standard deviation. The one-way ANOVA was applied to identify significance among the groups. The p value ≤0.05 was considered to be statistically significant.

RESULTS

Mean body weight (gram) of treated mice

The mean body weight of sodium arsenite treated (02 and 03) groups have shown decreasing tendencyafter some days of treatment in comparison to control group (01) while T. cordifolia administered group as in 04 and 05 reflects a rise in the mean weight of animals when data are compared with corresponding value of sodium arsenite treated groups (fig. 1). The group 01(control) depicts uniformly increasing in weight.

Fig.1: Mean body weight of treated mice. The number of animals (n=5) in each group

Mean value of micronucleus/2000 cells scored

Micronuclei are defined chromatin corpuscles with a diameter less or equal to 1/3 of main cell nucleus and stained equally or lighter than the parent nucleus. The mean value of micronucleus is higher in group 02 and03 in respect to its number in group 04, 05 (as shown in fig. 2). The average number of micronucleus per 2000 cell was found to be 2.6, 19.2, 20.2,7 and 6.8 in group 01, 02, 03, 04, 05 respectively.

These obtained data can be compared with the few studies, in which herbal extract has anti-mutagenic and anti-clastogenic potential against a diverse kinds of clastogenic substances in context of bone marrow MN assay.Cyclophosphamide treated rat showed decrease in MN frequency after oral administration of methanolic bark extract of Ficusbenghalensis[21]. The Tinospora cordifolia methanolic stem extract retarded the MN formation in dose dependent manner in melanoma tumor model and have a preventive effect on volume of tumor against cyclophosphamide induced toxicity [22].

Fig. 2:Mean value of micronucleus in different experimental groups, each value in fig. was obtained by calculating the average of three experiments. The number of animals (n=5) in each group, Mean numbers of polychromatic erythrocytes (PCE) and normochromatic erythrocytes (NCE) with micronucleus (MN)

Fig.3:Mean value of micro nucleatedpolychromatic erythrocytes (MNPCE) and micronucleatednormochromatic erythrocytes (MNCE) in different experimental groups.Each value in fig. was obtained by calculating the average of three experiments. The number of animals (n=5) in each group

Table1: Mean and standard deviation of micronucleus frequency in bone marrow of mice

Group Treatment Dose (mg/kg body weight) % frequency of MN(mean±sd)
01 Tap water 0 0.13±0.02449
02 Sodium arsenite 4 0.80±0.34205*
03 4
  1. ±0.10198

04 T. cordifoliastem extract 80 0.35±0.07071**
05 0.34±0.13928***

sd: Standard deviation.MN: Micronucleus. T. cordifolia: Tinospora cordifolia.Each value in table was obtained by calculating the average of three experiments.*p≤ 0.002, comparedto the corresponding value for controlanimals (Group 01).**p≤0.019, compared to the corresponding value for arsenic treated animals (Group 02).***p≤0.001, compared to the corresponding value for arsenic treated animals (Group 03).

Determination of percentage frequency of micronucleus by mean and standard deviation

Percentage frequencies of micronucleus were used to assess genotoxicity caused by arsenicals as well as evaluation of the anticlastgenic potential of test plant. It is calculated by using a simple formula: % MN frequency = (number of micronucleus/number of total cells scored) × 100.

After oral administration of sodium arsenite to mice (Groups 02,03)caused marked elevations of micronuclei frequency in bone marrow cells as presented in table 1. Group02 showed significantly (p≤0.002) rise in MN frequency when compared to the Control(group 01) and (p≤ 0.001) when group 03 was compared to the corresponding value for control animal. But there was a sharp decrease in MN frequency in arsenite pre-treated groups (04, 05) after treatment of test plant stem extract. Tinospora cordifolia stem extract treated mice (04) showed notable (p ≤0.019) decline in micronucleus frequency,when compared to the corresponding value for group 02 animals whilegroup 05showed significant (p≤0.001) decline when data were compared with arsenic treated group 03.

Fig.4:Microphotograph (A--C) showing micro nucleated PCE and NCE at magnification (10 × 100) under oil immersion

DISCUSSION

All chemicals those produce chromatin material damage leading to generation of MN or mutation are regarded as genotoxic. The bone marrow MN assay is one of the most suitable genotoxic tests [23]. Increase in the percentage frequency of micronucleus in the arsenite treated animals is an indication of chromosomal damages. There are several ways of arsenic toxicity but generation of free radical has prime importance in toxicity or clastogenicity of chromatin materials. Antioxidant therapy is vital in scavenging free radicals; plant derived antioxidants is capable to checkthe formation of free radicals, which reacts with bio-molecules like DNA and Proteins[24]. Free radicals are mainly oxygen molecules or atoms having an unpaired electron in their outermost orbit [25].Arsenicals are well known clastogen which induces micronuclei formation (as shown in fig. 4).T. cordifoliashows anticlastogenic potential against arsenical genotoxicity to a great extent. This was confirmed by present investigation and data analysis which depicts that frequency of micronuclei was drastically decreased in those animal groups which were treated with the test plant stem extract. This may probably happened due to the antagonisticeffect of this herb which facilitates repairing action of chromatin material. The mean number of micronucleus and their percentage frequency (mean±standard deviation) were falling down in group 04 and 05 in comparison to group 02, 03. Animals of group 02 and 03 received sodium arsenite alone while group 04, 05 were received ethanolic stem extract of the test plant after exposure of sodium arsenite.ThusT. cordifolia may have a good anticlastogenic effect on arsenic induced genotoxicity.

CONCLUSION

Arsenical mainly promotes micronuclei formation via clastogenic or aneugenic mechanism and also causes DNA breakdown due to generation of reactive oxygen species. The present investigation has shown that thetest plant stemextract may have anti-mutagenic oranticlastgenic property so it is noteworthy in the preventive aspects of chemical carcinogenesis andseveral types ofdisorders caused by genetic damages due to arsenic toxicity.The findings of this study have concluded thatT. cordifolia may be used as a preventive herbal drug against chemical or arsenictoxicity.

ACKNOWLEDGMENT

The study was financially supported by DST,Government of India, under project DBT-PU-IPLS, Sanction No: BT/PR4577/INF/22/149/2012.

AUTHOR CONTRIBUTION

All authors had equally contributed the research work

CONFLICT OF INTERESTS

The authors have declared no conflict of interest

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How to cite this article

  • SK Ambasta, S Kumari, UK Sinha. Anticlastogenicity of Tinospora cordifolia stem extract against arsenic genotoxicity in Mus musculus bone marrow erythrocytes using micronucleus assay.Int J Pharm Pharm Sci 2017;9(10):260-264.



About this article

Title

ANTICLASTOGENICITY OF TINOSPORA CORDIFOLIA STEM EXTRACT AGAINST ARSENIC GENOTOXICITY IN MUS MUSCULUS BONE MARROW ERYTHROCYTES USING MICRONUCLEUS ASSAY

Keywords

Acentromeric, Mitotic apparatus, Genotoxicity

DOI

10.22159/ijpps.2017v9i10.20249

Date

02-10-2017

Additional Links

Manuscript Submission

Journal

International Journal of Pharmacy and Pharmaceutical Sciences
Vol. 9, Issue 10, 2017 Page: 260-264

Online ISSN

0975-1491

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Authors & Affiliations

S. K. Ambasta
Department of Botany (Biotechnology), Faculty of Science, Patna University, Patna, Bihar, India
India

S. Kumari
Department of Biotechnology, Faculty of Science, Utkal University, Bhubaneswar, Odisha, India
India

Uk Sinha
Department of Botany (Biotechnology), Faculty of Science, Patna University, Patna, Bihar, India


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